# FDA recall Z-0972-2024

> **THOR Photomedicine Ltd** · Class II · device recall initiated 2023-11-20.

## Product

NovoTHOR Whole Body Light Pod, Gen 3.0    (1) Product Code S2188 - Reg  (2) Product Code S2189 - Reg PRX  (3) Product Code S2190 - XL

## Reason for recall

One of the ball studs attaching a gas strut to the canopy may fail. There is potential risk of injury should a ball stud fail when someone is in the NovoTHOR and trying to open or close the canopy

## Distribution

Domestic distribution to the states of Arizona California Colorado Connecticut Florida Georgia Hawaii Idaho Indiana Maryland New Jersey New York Oregon Pennsylvania Texas Washington Wisconsin.  Foreign distribution to Australia, Canada, Italy, Malta, Norway, Switzerland, UAE, and UK.

## Key facts

- **Recall number:** Z-0972-2024
- **Recalling firm:** THOR Photomedicine Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-20
- **Report date:** 2024-02-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Amersham, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0972-2024

## Citation

> AI Analytics. FDA recall Z-0972-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0972-2024. Source: US FDA. Licensed CC0.

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